Fluoxetine (Prozac) interaction with the mitochondrial voltage-dependent anion channel and protection against apoptotic cell death

被引:83
作者
Nahon, E [1 ]
Israelson, A [1 ]
Abu-Hamad, S [1 ]
Shoshan-Barmatz, V [1 ]
机构
[1] Ben Gurion Univ Negev, Dept Life Sci, IL-84105 Beer Sheva, Israel
来源
FEBS LETTERS | 2005年 / 579卷 / 22期
基金
以色列科学基金会;
关键词
voltage-dependent anion channel; fluoxetine; Prozac; permeability transition pore; apoptosis; cytochrome c;
D O I
10.1016/j.febslet.2005.08.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fluoxetine (Prozac) is a potent antidepressant compound inhibiting serotonin reuptake, but also Na+, K+ and Ca2+ channels and reported to both trigger and prevent apoptosis. Recently, fluoxetine was found to increase the voltage sensitivity of the mitochondrial voltage-dependent anion channel (VDAC). VDAC which functions in transporting metabolites across the mitochondria also plays a crucial role in apoptosis. Here, we demonstrate that fluoxetine interacted with VDAC and decreased its conductance. Fluoxetine inhibited the opening of the mitochondrial permeability transition pore, the release of cytochrome c, and protected against staurosporine-induced apoptotic cell death. These findings may explain some of the reported fluoxetine side effects. (c) 2005 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:5105 / 5110
页数:6
相关论文
共 34 条
  • [1] In self-defence: Hexokinase promotes voltage-dependent anion channel closure and prevents mitochondria-mediated apoptotic cell death
    Azoulay-Zohar, H
    Israelson, A
    Abu-Hamad, S
    Shoshan-Barmatz, V
    [J]. BIOCHEMICAL JOURNAL, 2004, 377 : 347 - 355
  • [2] Side-effect profile of Fluoxetine in comparison with other SSRIs, tricyclic and newer antidepressants: A meta-analysis of clinical trial data
    Brambilla, P
    Cipriani, A
    Hotopf, M
    Barbui, C
    [J]. PHARMACOPSYCHIATRY, 2005, 38 (02) : 69 - 77
  • [3] BRANDES LJ, 1992, CANCER RES, V52, P3796
  • [4] The voltage-dependent anion channel is the target for a new class of inhibitors of the mitochondrial permeability transition pore
    Cesura, AM
    Pinard, E
    Schubenel, R
    Goetschy, V
    Friedlein, A
    Langen, H
    Polcic, P
    Forte, MA
    Bernardi, P
    Kemp, JA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (50) : 49812 - 49818
  • [5] VDAC: The channel at the interface between mitochondria and the cytosol
    Colombini, M
    [J]. MOLECULAR AND CELLULAR BIOCHEMISTRY, 2004, 256 (1-2) : 107 - 115
  • [6] Cotterchio M, 2000, AM J EPIDEMIOL, V151, P951, DOI 10.1093/oxfordjournals.aje.a010138
  • [7] The mitochondrial permeability transition pore and its role in cell death
    Crompton, M
    [J]. BIOCHEMICAL JOURNAL, 1999, 341 : 233 - 249
  • [8] Fluoxetine interacts with the lipid bilayer of the inner membrane in isolated rat brain mitochondria, inhibiting electron transport and F1F0-ATPase activity
    Curti, C
    Mingatto, FE
    Polizello, ACM
    Galastri, LO
    Uyemura, SA
    Santos, AC
    [J]. MOLECULAR AND CELLULAR BIOCHEMISTRY, 1999, 199 (1-2) : 103 - 109
  • [9] Inhibition of voltage-gated calcium channels by fluoxetine in rat hippocampal pyramidal cells
    Deák, F
    Lasztóczi, B
    Pacher, P
    Petheö, GL
    Kecskeméti, V
    Spät, A
    [J]. NEUROPHARMACOLOGY, 2000, 39 (06) : 1029 - 1036
  • [10] Opening of plasma membrane voltage-dependent anion channels (VDAC) precedes caspase activation in neuronal apoptosis induced by toxic stimuli
    Elinder, F
    Akanda, N
    Tofighi, R
    Shimizu, S
    Tsujimoto, Y
    Orrenius, S
    Ceccatelli, S
    [J]. CELL DEATH AND DIFFERENTIATION, 2005, 12 (08) : 1134 - 1140